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CCR7 定义了胸腺和外周血中鼠类 iNKT 细胞的前体细胞。

CCR7 defines a precursor for murine iNKT cells in thymus and periphery.

机构信息

The Department of Laboratory Medicine and Pathology, Center for Immunology, University of Minnesota, Minneapolis, United States.

出版信息

Elife. 2018 Aug 13;7:e34793. doi: 10.7554/eLife.34793.

Abstract

The precise steps of iNKT subset differentiation in the thymus and periphery have been controversial. We demonstrate here that the small proportion of thymic iNKT and mucosal associated invariant T cells that express CCR7 represent a multi-potent progenitor pool that gives rise to effector subsets within the thymus. Using intra-thymic labeling, we also showed that CCR7 iNKT cells emigrate from the thymus in a dependent manner, and undergo further maturation after reaching the periphery. deficiency impaired differentiation of iNKT effector subsets and localization to the medulla. Parabiosis and intra-thymic transfer showed that thymic NKT1 and NKT17 were resident-they were not derived from and did not contribute to the peripheral pool. Finally, each thymic iNKT effector subset produces distinct factors that influence T cell development. Our findings demonstrate how the thymus is both a source of iNKT progenitors and a unique site of tissue dependent effector cell differentiation.

摘要

NKT 亚群在胸腺和外周中的分化的确切步骤一直存在争议。我们在这里证明,表达 CCR7 的胸腺和黏膜相关不变 T 细胞中的一小部分 NKT 细胞代表了一个多能祖细胞池,可在外周中产生效应子亚群。通过胸腺内标记,我们还表明 CCR7+iNKT 细胞依赖于 依赖性从胸腺中迁出,并在到达外周后进一步成熟。缺陷可损害 iNKT 效应子亚群的分化和向皮质的定位。联体共生和胸腺内转移表明,胸腺中的 NKT1 和 NKT17 是驻留的——它们不是来自于外周池,也不对外周池做出贡献。最后,每个胸腺内的 iNKT 效应子亚群都会产生影响 T 细胞发育的独特因子。我们的研究结果表明,胸腺既是 NKT 祖细胞的来源,也是组织依赖的效应细胞分化的独特部位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c456/6115192/9c3cf38c8ed1/elife-34793-fig1.jpg

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